• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基质金属蛋白酶-1组织抑制剂敲低抑制人脂肪来源干细胞的增殖。

Tissue Inhibitor of Matrix Metalloproteinases-1 Knockdown Suppresses the Proliferation of Human Adipose-Derived Stem Cells.

作者信息

Zhang Peihua, Li Jin, Qi Yawei, Tang Xudong, Duan Jianfeng, Liu Li, Wu Zeyong, Liang Jie, Li Jiangfeng, Wang Xian, Zeng Guofang, Liu Hongwei

机构信息

Institute of Plastic Surgery, Stem Cell Research and Clinical Translation Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524001, China.

Institute of Biochemistry and Molecular Biology, Guangdong Medical University, Zhanjiang, Guangdong 524023, China.

出版信息

Stem Cells Int. 2016;2016:4761507. doi: 10.1155/2016/4761507. Epub 2016 Apr 27.

DOI:10.1155/2016/4761507
PMID:27239203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4863124/
Abstract

Tissue inhibitor of metalloproteinases-1 (TIMP-1) is a multifunctional matrix metalloproteinase, and it is involved in the regulation of cell proliferation and apoptosis in various cell types. However, little is known about the effect of TIMP-1 expression on the proliferation of adipose-derived stem cells (ADSCs). Therefore, TIMP-1 expression in the ADSCs was firstly detected by western blotting, and TIMP-1 gene was knocked down by lentivirus-mediated shRNA. Cell proliferation was then evaluated by MTT assay and Ki67 staining, respectively. Cell cycle progression was determined by flow cytometry. The changes of p51, p21, cyclin E, cyclin-dependent kinase 2 (CDK2), and P-CDK2 caused by TIMP-1 knockdown were detected by western blotting. The results indicated that ADSCs highly expressed TIMP-1 protein, and the knockdown of TIMP-1 inhibited cell proliferation and arrested cell cycle progression at G1 phase in the ADSCs possibly through the upregulation of p53, p21, and P-CDK2 protein levels and concurrent downregulation of cyclin E and CDK2 protein levels. These findings suggest that TIMP-1 works as a positive regulator of cell proliferation in ADSCs.

摘要

金属蛋白酶组织抑制剂-1(TIMP-1)是一种多功能基质金属蛋白酶,参与多种细胞类型的细胞增殖和凋亡调控。然而,关于TIMP-1表达对脂肪来源干细胞(ADSCs)增殖的影响知之甚少。因此,首先通过蛋白质印迹法检测ADSCs中TIMP-1的表达,并通过慢病毒介导的短发夹RNA(shRNA)敲低TIMP-1基因。然后分别通过MTT法和Ki67染色评估细胞增殖。通过流式细胞术确定细胞周期进程。通过蛋白质印迹法检测TIMP-1敲低引起的p51、p21、细胞周期蛋白E、细胞周期蛋白依赖性激酶2(CDK2)和磷酸化CDK2的变化。结果表明,ADSCs高表达TIMP-1蛋白,TIMP-1的敲低抑制了ADSCs的细胞增殖,并可能通过上调p53、p21和磷酸化CDK2蛋白水平以及同时下调细胞周期蛋白E和CDK2蛋白水平使细胞周期进程停滞在G1期。这些发现表明,TIMP-1在ADSCs中作为细胞增殖的正调节因子发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/a0320d927c34/SCI2016-4761507.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/2d2e0aa198f5/SCI2016-4761507.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/b5a704325953/SCI2016-4761507.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/6db794e63672/SCI2016-4761507.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/c7799f02793b/SCI2016-4761507.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/58b780af0170/SCI2016-4761507.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/a0320d927c34/SCI2016-4761507.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/2d2e0aa198f5/SCI2016-4761507.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/b5a704325953/SCI2016-4761507.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/6db794e63672/SCI2016-4761507.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/c7799f02793b/SCI2016-4761507.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/58b780af0170/SCI2016-4761507.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89d9/4863124/a0320d927c34/SCI2016-4761507.006.jpg

相似文献

1
Tissue Inhibitor of Matrix Metalloproteinases-1 Knockdown Suppresses the Proliferation of Human Adipose-Derived Stem Cells.基质金属蛋白酶-1组织抑制剂敲低抑制人脂肪来源干细胞的增殖。
Stem Cells Int. 2016;2016:4761507. doi: 10.1155/2016/4761507. Epub 2016 Apr 27.
2
Vitamin C promotes the proliferation of human adipose-derived stem cells via p53-p21 pathway.维生素C通过p53-p21途径促进人脂肪来源干细胞的增殖。
Organogenesis. 2016 Jul 2;12(3):143-151. doi: 10.1080/15476278.2016.1194148. Epub 2016 May 26.
3
Down-regulation of long non-coding RNA MALAT1 inhibits granulosa cell proliferation in endometriosis by up-regulating P21 via activation of the ERK/MAPK pathway.长链非编码 RNA MALAT1 的下调通过激活 ERK/MAPK 通路上调 P21 抑制子宫内膜异位症中的颗粒细胞增殖。
Mol Hum Reprod. 2019 Jan 1;25(1):17-29. doi: 10.1093/molehr/gay045.
4
Adipose-derived stromal cells protect intervertebral disc cells in compression: implications for stem cell regenerative disc therapy.脂肪来源的基质细胞在压缩状态下保护椎间盘细胞:对干细胞再生椎间盘治疗的启示。
Int J Biol Sci. 2015 Jan 1;11(2):133-43. doi: 10.7150/ijbs.10598. eCollection 2015.
5
Protein kinase C delta inhibits Caco-2 cell proliferation by selective changes in cell cycle and cell death regulators.蛋白激酶Cδ通过细胞周期和细胞死亡调节因子的选择性变化抑制Caco-2细胞增殖。
Oncogene. 2006 May 25;25(22):3123-38. doi: 10.1038/sj.onc.1209360.
6
A novel all-trans retinoic acid derivative 4-amino‑2‑trifluoromethyl-phenyl retinate inhibits the proliferation of human hepatocellular carcinoma HepG2 cells by inducing G0/G1 cell cycle arrest and apoptosis via upregulation of p53 and ASPP1 and downregulation of iASPP.一种新型全反式维甲酸衍生物4-氨基-2-三氟甲基苯基维甲酸酯通过上调p53和ASPP1以及下调iASPP诱导G0/G1期细胞周期阻滞和凋亡,从而抑制人肝癌HepG2细胞的增殖。
Oncol Rep. 2016 Jul;36(1):333-41. doi: 10.3892/or.2016.4795. Epub 2016 May 9.
7
Overexpressed vascular endothelial growth factor in adipose derived stem cells attenuates fibroblasts and skin injuries by ultraviolet radiation.脂肪来源干细胞中过度表达的血管内皮生长因子可减轻紫外线辐射对成纤维细胞和皮肤的损伤。
Biosci Rep. 2019 Jul 18;39(7). doi: 10.1042/BSR20190433. Print 2019 Jul 31.
8
Inhibition of pancreatic stellate cell activity by adipose-derived stem cells.脂肪来源干细胞对胰腺星状细胞活性的抑制作用。
Hepatobiliary Pancreat Dis Int. 2015 Apr;14(2):215-21. doi: 10.1016/s1499-3872(14)60283-6.
9
[Effect of CDK2-AP1 gene over-expression on proliferation and cell cycle regulation of breast cancer cell line MCF-7].[CDK2-AP1基因过表达对乳腺癌细胞系MCF-7增殖及细胞周期调控的影响]
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2012 Oct;37(10):990-6. doi: 10.3969/j.issn.1672-7347.2012.10.004.
10
Knockdown of NANOG Reduces Cell Proliferation and Induces G0/G1 Cell Cycle Arrest in Human Adipose Stem Cells.敲低 NANOG 减少人脂肪干细胞的增殖并诱导 G0/G1 细胞周期停滞。
Int J Mol Sci. 2019 May 26;20(10):2580. doi: 10.3390/ijms20102580.

引用本文的文献

1
IgE Immune Complexes Mitigate Eosinophilic Immune Responses through NLRC4 Inflammasome.IgE 免疫复合物通过 NLRC4 炎性小体减轻嗜酸性免疫应答。
Mediators Inflamm. 2023 Oct 18;2023:3224708. doi: 10.1155/2023/3224708. eCollection 2023.
2
Regenerative Effect of Adipose Derived Mesenchymal Stem Cells on Ganglion Cells in the Hypoxic Organotypic Retina Culture.脂肪来源间充质干细胞对缺氧器官型视网膜培养物中神经节细胞的再生作用
Int J Stem Cells. 2023 May 30;16(2):244-249. doi: 10.15283/ijsc22041. Epub 2022 Dec 31.
3
RAB37 Promotes Adipogenic Differentiation of hADSCs via the TIMP1/CD63/Integrin Signaling Pathway.

本文引用的文献

1
Xenotransplantation of human adipose-derived stem cells in zebrafish embryos.人脂肪来源干细胞在斑马鱼胚胎中的异种移植。
PLoS One. 2015 Apr 7;10(4):e0123264. doi: 10.1371/journal.pone.0123264. eCollection 2015.
2
Adipose derived stem cells and nerve regeneration.脂肪来源干细胞与神经再生。
Neural Regen Res. 2014 Jul 15;9(14):1341-6. doi: 10.4103/1673-5374.137585.
3
Dynamic changes of matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 1 after burn injury.烧伤后基质金属蛋白酶 9 和金属蛋白酶组织抑制剂 1 的动态变化。
RAB37通过TIMP1/CD63/整合素信号通路促进人脂肪干细胞的成脂分化。
Stem Cells Int. 2021 Nov 23;2021:8297063. doi: 10.1155/2021/8297063. eCollection 2021.
4
SORLA is required for insulin-induced expansion of the adipocyte precursor pool in visceral fat.SORLA 对于胰岛素诱导内脏脂肪前体细胞库的扩增是必需的。
J Cell Biol. 2021 Dec 6;220(12). doi: 10.1083/jcb.202006058. Epub 2021 Nov 15.
5
Human adipose tissue-derived mesenchymal stem cells and their extracellular vesicles modulate lipopolysaccharide activated human microglia.人脂肪组织来源的间充质干细胞及其细胞外囊泡调节脂多糖激活的人小胶质细胞。
Cell Death Discov. 2021 May 10;7(1):98. doi: 10.1038/s41420-021-00471-7.
6
TIMP-1 downregulation modulates miR-125a-5p expression and triggers the apoptotic pathway.基质金属蛋白酶组织抑制因子-1的下调调节微小RNA-125a-5p的表达并触发凋亡途径。
Oncotarget. 2018 Jan 2;9(10):8941-8956. doi: 10.18632/oncotarget.23832. eCollection 2018 Feb 6.
J Crit Care. 2015 Feb;30(1):162-6. doi: 10.1016/j.jcrc.2014.07.008. Epub 2014 Jul 11.
4
Dihydromyricetin induces cell cycle arrest and apoptosis in melanoma SK-MEL-28 cells.二氢杨梅素诱导黑色素瘤 SK-MEL-28 细胞周期阻滞和凋亡。
Oncol Rep. 2014 Jun;31(6):2713-9. doi: 10.3892/or.2014.3160. Epub 2014 Apr 25.
5
A rapid and efficient method for primary culture of human adipose-derived stem cells.一种快速高效的人脂肪来源干细胞原代培养方法。
Organogenesis. 2013 Oct 1;9(4):287-95. doi: 10.4161/org.27153. Epub 2013 Nov 22.
6
siRNA knockdown of tissue inhibitor of metalloproteinase-1 in keloid fibroblasts leads to degradation of collagen type I.RNA 干扰技术下调瘢痕成纤维细胞中金属蛋白酶组织抑制剂-1 的表达导致 I 型胶原的降解。
J Invest Dermatol. 2014 Mar;134(3):818-826. doi: 10.1038/jid.2013.396. Epub 2013 Sep 16.
7
Enhancement of renal epithelial cell functions through microfluidic-based coculture with adipose-derived stem cells.通过与脂肪来源干细胞的基于微流控的共培养增强肾上皮细胞功能。
Tissue Eng Part A. 2013 Sep;19(17-18):2024-34. doi: 10.1089/ten.TEA.2012.0605. Epub 2013 Jul 5.
8
Overexpression of TIMP-1 in embryonic stem cells attenuates adverse cardiac remodeling following myocardial infarction.TIMP-1 在胚胎干细胞中的过表达可减轻心肌梗死后的心脏不良重构。
Cell Transplant. 2012;21(9):1931-44. doi: 10.3727/096368911X627561. Epub 2012 Mar 22.
9
Interferon Regulatory Factor 1 (IRF-1) induces p21(WAF1/CIP1) dependent cell cycle arrest and p21(WAF1/CIP1) independent modulation of survivin in cancer cells.干扰素调节因子 1(IRF-1)诱导细胞周期停滞依赖于 p21(WAF1/CIP1)和非依赖于 p21(WAF1/CIP1)的调节肿瘤细胞中的存活素。
Cancer Lett. 2012 Jun 1;319(1):56-65. doi: 10.1016/j.canlet.2011.12.027. Epub 2011 Dec 23.
10
Phosphorylation of MCM3 protein by cyclin E/cyclin-dependent kinase 2 (Cdk2) regulates its function in cell cycle.MCM3 蛋白的磷酸化由细胞周期蛋白 E/细胞周期依赖性激酶 2(Cdk2)调节,这调控了其在细胞周期中的功能。
J Biol Chem. 2011 Nov 18;286(46):39776-85. doi: 10.1074/jbc.M111.226464. Epub 2011 Sep 30.